# K102476: Teleradpro

- Pathway: 510(k) (Special)
- Applicant: Vidar Systems Corp.
- Decided: Oct 7, 2010 after 38 days
- Product code: LMA (Digitizer, Image, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K933632 (1993). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993597: PLLL, Teleradpro, Model 12714/12715, VXR-12 Plus, Model 8619/9617, Vidar Systems Corp. (1999) Summary page 1.

## Most influential descendants
- K130636: Teleradpro Edge; Teleradpro Edge HD-CCD (2013), 0 descendants of its own

## Indications for use
The TeleradPRO film digitizer is intended for making digital copies of medical x-ray films.

Source page: https://510kreport.com/device/K102476
Methodology: https://510kreport.com/methodology